| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:123654388-123654715 | Common:3; Rare:81; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:123741643-123741799 | Common:1; Rare:42 | ||||
| chr11:124622684-124622918 | Common:5; Rare:78 | ||||
| chr11:124673706-124673935 | Common:4; Rare:71 | ||||
| chr11:124762216-124762424 | Rare:56 | ||||
| chr11:124800662-124800740 | Common:1; Rare:11 | ||||
| chr11:124876594-124876869 | Common:2; Rare:53 | ||||
| chr11:124935932-124936076 | Common:1; Rare:36; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:124936124-124936142 | Rare:3 | ||||
| chr11:124936336-124936517 | Rare:30 | ||||
| chr11:124953945-124954215 | Common:5; Rare:78 | ||||
| chr11:125111710-125112032 | Common:3; Rare:67 | ||||
| chr11:125451523-125451625 | Rare:21 | ||||
| chr11:125495388-125495511 | Common:3; Rare:47 | ||||
| chr11:125495513-125495832 | Common:3; Rare:71 |